The following data is part of a premarket notification filed by Medicult A/s with the FDA for Biopsy Medium, Model Ref 1062.
Device ID | K060983 |
510k Number | K060983 |
Device Name: | BIOPSY MEDIUM, MODEL REF 1062 |
Classification | Media, Reproductive |
Applicant | MEDICULT A/S 9915 CAM. CHIRIMOLLA San Diego, CA 92131 |
Contact | Ronald G Leonardi |
Correspondent | Ronald G Leonardi MEDICULT A/S 9915 CAM. CHIRIMOLLA San Diego, CA 92131 |
Product Code | MQL |
CFR Regulation Number | 884.6180 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-04-10 |
Decision Date | 2006-07-28 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00888937800654 | K060983 | 000 |